A. Wigger et al., Nonresponsiveness of the rat hypothalamo-pituitary-adrenocortical axis to parturition-related events: Inhibitory action of endogenous opioids, ENDOCRINOL, 140(6), 1999, pp. 2843-2849
During the last 2 days of pregnancy in rats, basal corticosterone secretion
is enhanced, although the response of the hypothalamo-pituitary-adrenocort
ical (HPA) axis to emotional and physical stressors is blunted, independent
of the action of endogenous opioids. In this study, alterations in the rea
ctivity of the HPA axis, which may accompany parturition-related stimuli, a
nd the involvement of endogenous opioids were examined in chronically cathe
terized rats.
In vehicle-treated controls (n = 9), ACTH and corticosterone secretion decr
eased in preparation for birth (P < 0.01) and further declined immediately
after delivery of the second pup (P < 0.01), remaining low for 150 min. In
contrast, in animals injected with the opiate antagonist naloxone (5 mg ml(
-1) kg(-1), iv, n = 6) after delivery of the second pup, ACTH and corticost
erone release were enhanced within 20 min (ACTH, 5.0-fold; corticosterone,
2.3-fold; P < 0.01 vs. controls) and returned to control levels after 90 mi
n. In confirmation of previous reports, oxytocin secretion into blood was e
levated in control rats after the onset of parturition (P < 0.01) and was f
urther enhanced in the naloxone group (1.4-fold, P < 0.01 vs. control). Pla
sma lactate concentration was increased, 30 min aff er the onset of deliver
y (1.9-fold, P < 0.01), independent of the treatment. The data indicate tha
t parturition-related events do not trigger HPA axis hormone release becaus
e of an effective inhibition by endogenous opioids. This nonresponsiveness
of the HPA axis is likely to protect the pups' well-being during birth.